				Excel File Text File All mouse models of peroxisomal disease with phenotypic similarity to the human disease
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
				alpha-methylacyl-CoA racemase deficiency	Amacrtm1Jkh/Amacrtm1Jkh	involves: 129S1/Sv * 129X1/SvJ	J:90370	View
				D-bifunctional protein deficiency	Ehhadhtm1Jkr/Ehhadhtm1Jkr Hsd17b4tm1Baes/Hsd17b4tm1Baes	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J	J:89945, J:99925	View
				D-bifunctional protein deficiency	Hsd17b4tm1Baes/Hsd17b4tm1Baes	involves: 129S1/Sv * 129X1/SvJ	J:62314, J:99925	View
				glutaric acidemia type 3	Sugcttm1.2Kald/Sugcttm1.2Kald	B6.Cg-Sugct^tm1.2Kald	J:293423	View
				peroxisomal acyl-CoA oxidase deficiency	Acox1tm1Jkr/Acox1tm1Jkr	involves: 129P2/OlaHsd * C57BL/6J	J:35794	View
				peroxisomal disease	Acbd5tm1a(EUCOMM)Wtsi/Acbd5tm1a(EUCOMM)Wtsi	C57BL/6N-A^tm1Brd Acbd5^{tm1a(EUCOMM)Wtsi}/WtsiCnbc	J:299448	View
				Zellweger syndrome	Pex1tm1.1Hrw/Pex1tm1.1Hrw	involves: C57BL/6NTac	J:278655	View
				Zellweger syndrome	Pex1tm1.1Sjms/Pex1tm1.1Sjms	involves: 129 * C57BL/6N	J:210296	View
				Zellweger syndrome	Pex11btm1Sjg/Pex11b+	B6.129-Pex11b^tm1Sjg	J:180632	View
				Zellweger syndrome	Pex11btm1Sjg/Pex11btm1Sjg	B6.129-Pex11b^tm1Sjg	J:180632	View
				Zellweger syndrome	Pex11btm1Sjg/Pex11btm1Sjg	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:76782	View

				No similarity to the expected human disease phenotype was found.
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
NOT Models				acatalasia	Catb/Catb	Not Specified	J:105024	View